chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154164297941642980CT44GENICpossibly homozygous112808579
154164310741643108CT60GENIChomozygous112491403
154164323741643238CT49GENIChomozygous112491405
154164324941643250GA52GENIChomozygous112491407
154164326041643261CG50GENIChomozygous112491409
154164486241644863AG50GENIChomozygous112491411